Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
Source | Last Updated |
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Alliance of Genome Resources | October 9, 2024 |
Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▲ | FlyGlycoDB | Evidence Code Names | References |
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DOID:5844 | myocardial infarction | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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DOID:10763 | hypertension | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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DOID:0060041 | autism spectrum disorder | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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DOID:3021 | acute kidney failure | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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DOID:4724 | brain edema | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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DOID:7004 | ACTH-secreting pituitary adenoma | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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DOID:3829 | pituitary adenoma | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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DOID:0112121 | nephrogenic syndrome of inappropriate antidiuresis | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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DOID:3324 | mood disorder | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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DOID:3312 | bipolar disorder | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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DOID:12387 | nephrogenic diabetes insipidus | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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DOID:5419 | schizophrenia | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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DOID:1591 | renovascular hypertension | WB:WBGene00008808 | Caenorhabditis elegans | 184471 | ntr-2 |
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DOID:83 | cataract | WB:WBGene00003828 | Caenorhabditis elegans | 181174 | nuc-1 |
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DOID:7148 | rheumatoid arthritis | WB:WBGene00003828 | Caenorhabditis elegans | 181174 | nuc-1 |
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DOID:0080553 | congenital disorder of glycosylation Iaa | ZFIN:ZDB-GENE-040718-48 | Danio rerio (zebrafish) | 436629 | nus1 |
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DOID:0080227 | autosomal dominant intellectual developmental disorder 55 | ZFIN:ZDB-GENE-040718-48 | Danio rerio (zebrafish) | 436629 | nus1 |
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DOID:14330 | Parkinson's disease | ZFIN:ZDB-GENE-040718-48 | Danio rerio (zebrafish) | 436629 | nus1 |
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DOID:1826 | epilepsy | ZFIN:ZDB-GENE-040718-48 | Danio rerio (zebrafish) | 436629 | nus1 |
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DOID:5212 | congenital disorder of glycosylation | ZFIN:ZDB-GENE-040718-48 | Danio rerio (zebrafish) | 436629 | nus1 |
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DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | WB:WBGene00020679 | Caenorhabditis elegans | 177235 | ogdh-1 |
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DOID:0081326 | oxoglutarate dehydrogenase deficiency | WB:WBGene00020679 | Caenorhabditis elegans | 177235 | ogdh-1 |
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DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | WB:WBGene00014098 | Caenorhabditis elegans | 179674 | ogdh-2 |
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DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | WB:WBGene00014098 | Caenorhabditis elegans | 179674 | ogdh-2 |
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DOID:0081326 | oxoglutarate dehydrogenase deficiency | Xenbase:XB-GENE-1010765 | Xenopus laevis (African clawed frog) | 399021 | ogdh.S |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024